Tri-split face study of skin resurfacing modalities for the treatment of melasma, comparing
the medium depth trichloroacetic acid peel, CO2 laser and Qs-NdYag laser.
Drug: 22% TCA peel
Device: CO2 laser
Device: Qs-NdYag laser
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Full eligibility criteria for NCT02892071
Ages eligible for Study
20 Years to 60 Years
Genders eligible for Study
Accepts Healthy Volunteers
male or female participants
20 to 60 years old
participants with melasma on forehead and both cheeks
participants who failed topical therapy for melasma
participants who have never tried other therapies for melasma
use of oral contraceptive (OCP) within 3 months of starting the study
hormonal therapy within 3 months of starting the study
hormonal intrauterine device (IUD) within 3 months of starting the study
history of poor wound healing or abnormal scarring
history of lip or face herpes simplex virus infections
active facial skin infection
history of connective tissue disorders (such as lupus or scleroderma)
history of isotretinoin therapy within 6 months of starting the study
history of chemical peels, dermabrasion, laser therapy or intense pulse light (IPL) within 6 months before enrollment into the study
All locations for NCT02892071
View full eligibility
Tris trial is registered with FDA with number: NCT02892071. The sponsor of the trial is SUZAN OBAGI and it is looking for 20 volunteers for the current phase.
Official trial title: Tri-split Face Study of Skin Resurfacing Modalities for the Treatment of Melasma
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